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It was then reviewed for a second time and, after the result was confirmed internally, the sample was disposed of because the laboratory considered it unsafe for staff to handle

Canadian pharmacy brands undergo review ensuring bioequivalence to reference products, though individual response to vehicle ingredients like propylene glycol varies

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Therefore, we finalized a policy for CY 2025 and subsequent years (89 FR 93932 through 93938), to not package payment for cell and gene therapies into C-APCs, when those cell and gene therapies are not functioning as integral, ancillary, supportive, dependent, or adjunctive to the primary C-APC service